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Showing 1–27 of 27 results
Advanced filters: Author: Phoebe A Rice Clear advanced filters
  • The structure of the bacteriophage transposase MuA bound to DNA sequences that mimic both the transposon ends and the target DNA ends is solved; the picture of this synaptic complex illustrates the intricacy of Mu transposition, and exposes the architectural diversity among DDE recombinases in complex with substrate DNAs.

    • Sherwin P. Montaño
    • Ying Z. Pigli
    • Phoebe A. Rice
    Research
    Nature
    Volume: 491, P: 413-417
  • Base lesions can be directly repaired by oxidative dealkylation catalysed by AlkB in bacteria and by ABH2/ABH3 in man. Several structures of AlkB and ABH2 bound to dsDNA are solved. These structures reveal why AlkB prefers ssDNA to dsDNA substrates, and how ABH2 differs structurally, to allow it to repair dsDNA.

    • Cai-Guang Yang
    • Chengqi Yi
    • Chuan He
    Research
    Nature
    Volume: 452, P: 961-965
  • An analysis of 24,202 critical cases of COVID-19 identifies potentially druggable targets in inflammatory signalling (JAK1), monocyte–macrophage activation and endothelial permeability (PDE4A), immunometabolism (SLC2A5 and AK5), and host factors required for viral entry and replication (TMPRSS2 and RAB2A).

    • Erola Pairo-Castineira
    • Konrad Rawlik
    • J. Kenneth Baillie
    ResearchOpen Access
    Nature
    Volume: 617, P: 764-768
  • A screen utilizing an environmental DNA library in Escherichia coli is used to identify Brig1, a previously unknown anti-phage defence system with homologues across distinct clades of bacteria.

    • Amer A. Hossain
    • Ying Z. Pigli
    • Luciano A. Marraffini
    ResearchOpen Access
    Nature
    Volume: 629, P: 410-416
  • A global network of researchers was formed to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity; this paper reports 13 genome-wide significant loci and potentially actionable mechanisms in response to infection.

    • Mari E. K. Niemi
    • Juha Karjalainen
    • Chloe Donohue
    ResearchOpen Access
    Nature
    Volume: 600, P: 472-477
  • Dietary shifts are among the most important actions we can take to reduce the environmental impact of our food system and improve human health. However, implementing such changes requires that dietary recommendations be tailored to the cultural heritage, values and preferences of populations.

    • Brent Loken
    • Murli Dhar
    • Nancy Phoebe Rapando
    News & Views
    Nature Food
    Volume: 5, P: 723-724
  • A mitochondrial-targeted acyl protein thioesterase inhibitor enables the identification of ABHD10 as a mitochondrial S-depalmitoylase that acts on the nucleophilic active site residue of peroxiredoxin-5 to modulate its antioxidant capacity.

    • Yang Cao
    • Tian Qiu
    • Bryan C. Dickinson
    Research
    Nature Chemical Biology
    Volume: 15, P: 1232-1240
  • CRISPR–Cas is a bacterial defence system that can attack invading DNA to protect host cells, or help to insert DNA safely into the genome. Structures of this latter type of CRISPR–Cas system have now been visualized.

    • Orsolya Barabas
    • Phoebe A. Rice
    News & Views
    Nature
    Volume: 613, P: 634-635
  • Whole-genome sequencing, transcriptome-wide association and fine-mapping analyses in over 7,000 individuals with critical COVID-19 are used to identify 16 independent variants that are associated with severe illness in COVID-19.

    • Athanasios Kousathanas
    • Erola Pairo-Castineira
    • J. Kenneth Baillie
    ResearchOpen Access
    Nature
    Volume: 607, P: 97-103
  • Picornaviruses use modular RNA domains in their internal ribosome entry sites (IRESs) for translation through non-canonical, cap-independent mechanisms. Here the authors report the crystal structure of domain V from the IRES of hepatitis A virus (HAV) ssRNA genome, suggesting that the functional homology among different types of picornaviral IRESs is structure-based.

    • Deepak Koirala
    • Yaming Shao
    • Joseph A. Piccirilli
    ResearchOpen Access
    Nature Communications
    Volume: 10, P: 1-13
  • One of the conserved proteins of the Staphylococcus aureus mobile genomic island responsible for methicillin resistance is an active MCM-like helicase, thus suggesting replication that would enhance the efficiency of horizontal gene transfer.

    • Ignacio Mir-Sanchis
    • Christina A Roman
    • Phoebe A Rice
    Research
    Nature Structural & Molecular Biology
    Volume: 23, P: 891-898
  • Spinach is an RNA aptamer analog of GFP that is widely used for fluorescent labeling of cellular RNAs. Crystal structures of Spinach–fluorophore complexes uncover an unusual G-quadruplex RNA fold that is involved in ligand recognition and tuning of Spinach fluorescence properties.

    • Hao Huang
    • Nikolai B Suslov
    • Joseph A Piccirilli
    Research
    Nature Chemical Biology
    Volume: 10, P: 686-691
  • Crystal structures of the full-length VS ribozyme show a domain-swapped dimer that reveals potential mechanisms for cis and trans processing, and suggest convergent evolution in the active site motifs across multiple ribozymes.

    • Nikolai B Suslov
    • Saurja DasGupta
    • Joseph A Piccirilli
    Research
    Nature Chemical Biology
    Volume: 11, P: 840-846
  • A series of new cryo-EM structures reveals a surprising twist in how the RAG complex initiates V(D)J recombination. The initial complex with substrate DNA adopts two conformations: in one, the DNA is relatively undistorted but the scissile phosphate is far from the active site, and in the other the DNA is partially melted and unwound by half a turn, which allows the scissile phosphate to dock into the active site. Similar pre-catalysis DNA melting may occur with other DDE recombinases, for which equivalent complexes with uncleaved substrate DNA are not yet available.

    • Fred Dyda
    • Phoebe A. Rice
    News & Views
    Nature Structural & Molecular Biology
    Volume: 25, P: 648-649
  • The Somatic Mosaicism across Human Tissues Network aims to create a reference catalogue of somatic mosaicism across different tissues and cells within individuals.

    • Tim H. H. Coorens
    • Ji Won Oh
    • Yuqing Wang
    Reviews
    Nature
    Volume: 643, P: 47-59
  • Normally, expression of bacterial DNA damage repair genes is repressed by the binding of LexA protein to SOS ‘boxes’ in their operators. DNA damage activates the RecA protein, which promotes autocleavage of LexA such that its repression is relieved and repair proteins are expressed. These authors solve several structures of LexA dimer bound to SOS box DNA, and find that the orientation of the DNA-binding wings can account for the strict intersite spacing.

    • Adrianna P. P. Zhang
    • Ying Z. Pigli
    • Phoebe A. Rice
    Research
    Nature
    Volume: 466, P: 883-886
  • Two long-awaited structures of serine and tyrosine site-specific recombinases bound to DNA show how reactions that are basically the same can be carried out in surprisingly different ways.

    • Phoebe A Rice
    News & Views
    Nature Structural & Molecular Biology
    Volume: 12, P: 641-643